IQVIA Hiring Clinical Site Activation Coordinator

IQVIA Hiring Site Activation Coordinator | Clinical Research Role | Bengaluru Hybrid Job

IQVIA is hiring for the position of Site Activation Coordinator in Bengaluru with a hybrid work model. This is a strong opportunity for candidates with around 1 year of experience in clinical research or healthcare environments to build a career in clinical trial start-up, regulatory submissions, and site activation processes.

The company is offering multiple openings for this role within its global clinical operations team. This position is ideal for life sciences graduates looking to grow in clinical research, regulatory affairs, and clinical trial management.

Company Overview

IQVIA is a global leader in clinical research services, healthcare analytics, and life sciences consulting. The organization supports pharmaceutical, biotechnology, and medical device companies in accelerating drug development and improving patient outcomes.

With expertise in clinical trials, data science, and regulatory processes, IQVIA offers professionals exposure to global studies, international regulatory frameworks, and advanced clinical operations.

Job Role & Responsibilities

As a Site Activation Coordinator, you will support clinical trial start-up activities and ensure timely regulatory approvals and site readiness.

Key responsibilities include:

• Perform site activation activities for clinical studies under supervision
• Prepare and review regulatory documents for accuracy and completeness
• Support submission of documents to ethics committees and regulatory authorities
• Track and manage site activation timelines and deliverables
• Maintain internal systems, databases, and tracking tools
• Coordinate with project teams, site activation managers, and stakeholders
• Review and manage Informed Consent Forms (ICF) and Investigator Pack (IP) documents
• Follow up on approvals, document execution, and regulatory progress

This role plays a crucial part in ensuring smooth clinical trial initiation and compliance with global regulatory standards.

Eligibility / Qualifications

Candidates must meet the following educational requirements:

BSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research

Skills Required:

• Basic understanding of clinical trials and drug development process
• Knowledge of regulatory documentation and SOPs
• Strong attention to detail and organizational skills
• Good communication and interpersonal skills
• Proficiency in MS Office tools

Experience:

• Minimum 1 year experience in clinical research or healthcare environment

Location & Salary

• Location: Bengaluru (Hybrid Work Model)
• Salary: Competitive salary as per clinical research industry standards

Application Process

Interested candidates can apply through the official IQVIA careers portal:

Apply Here: https://jobs.iqvia.com/en/jobs/R1532119-0

Apply early as clinical research roles are highly competitive.

Frequently Asked Questions (FAQs)

Is this role suitable for freshers?

No, at least 1 year of relevant experience is required.

What does a Site Activation Coordinator do?

They manage regulatory documentation and site readiness for clinical trials.

Is this a clinical trial role?

Yes, it is part of clinical trial start-up and regulatory processes.

What is ICF and IP?

ICF is Informed Consent Form, and IP is Investigator Pack used in clinical trials.

What is the career growth?

You can grow into roles like Site Activation Specialist, Clinical Project Manager, or CRA.

---

Category	Details
Company	IQVIA
Vacancies	Site Activation Coordinator
Required Education	BSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research
Experience	1 Year